Enrollment Study Protocol Specified
Item
participants must be enrolled in partners protocol # 2008p000540 "prospective analysis of symptoms, functionality and quality of life questionnaires to evaluate lymphedema in patients following treatment for breast cancer"
boolean
C1516879 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Cording
Item
confirmed case of cording by a medical provider (physician, nurse practitioner, physician assistant)
boolean
C3698497 (UMLS CUI [1])
Age
Item
participants must be at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of greater than 1 year.
boolean
C0023671 (UMLS CUI [1])
Informed Consent
Item
ability to understand and the willingness to sign a written informed consent document.
boolean
C0021430 (UMLS CUI [1])
Compliance behavior Follow-up | Other Coding | Compliance behavior Clinic Visits
Item
willingness to comply with required follow up perometer measurements and clinical visits.
boolean
C1321605 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C3846158 (UMLS CUI [2])
C1321605 (UMLS CUI [3,1])
C0008952 (UMLS CUI [3,2])
Lacking Enrollment Study Protocol Specified | Patient withdrawn from Study Protocol Specified
Item
participants who are not enrolled or have been removed from partners protocol #
boolean
C0332268 (UMLS CUI [1,1])
C1516879 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C0205369 (UMLS CUI [1,4])
C0422727 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C0205369 (UMLS CUI [2,3])
ID.8
Item
2008p000540 will be excluded from this trial.
boolean
Metastatic malignant neoplasm to brain | Rationale Prognosis bad | Rationale Development Neurologic Dysfunction Progressive | Rationale Interference Evaluation
Item
participants with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.
boolean
C0220650 (UMLS CUI [1])
C2699007 (UMLS CUI [2,1])
C0278252 (UMLS CUI [2,2])
C2699007 (UMLS CUI [3,1])
C0243107 (UMLS CUI [3,2])
C0751377 (UMLS CUI [3,3])
C0205329 (UMLS CUI [3,4])
C2699007 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C1261322 (UMLS CUI [4,3])
Operative procedure on head | Irradiation of head | Operation on neck | Irradiation of neck | Operative procedure on upper extremity | UPPER EXTREMITY RADIATION | Operation on trunk | Therapeutic radiology procedure Trunk
Item
history of prior surgery or radiation to the head, neck, upper limb, or trunk.
boolean
C0195772 (UMLS CUI [1])
C2064931 (UMLS CUI [2])
C0185773 (UMLS CUI [3])
C0746818 (UMLS CUI [4])
C0186318 (UMLS CUI [5])
C0749835 (UMLS CUI [6])
C0185774 (UMLS CUI [7])
C1522449 (UMLS CUI [8,1])
C0460005 (UMLS CUI [8,2])
Malignant Neoplasms | Exception Disease Free Duration | Exception Low Risk Recurrent tumor | Exception Carcinoma in situ of uterine cervix Treated | Exception Basal cell carcinoma Treated | Exception Squamous cell carcinoma of skin Treated
Item
patients with a history of a different malignancy are ineligible except for the following circumstances. individuals with a history of other malignancies are eligible if they have been disease-free for at least 5 years and are deemed by the investigator to be at low risk for recurrence of that malignancy. individuals with the following cancers are eligible if diagnosed and treated within the past 5 years: cervical cancer in situ, and basal cell or squamous cell carcinoma of the skin.
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])
C0332296 (UMLS CUI [2,3])
C0449238 (UMLS CUI [2,4])
C1705847 (UMLS CUI [3,1])
C3538919 (UMLS CUI [3,2])
C0521158 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0851140 (UMLS CUI [4,2])
C1522326 (UMLS CUI [4,3])
C1705847 (UMLS CUI [5,1])
C0007117 (UMLS CUI [5,2])
C1522326 (UMLS CUI [5,3])
C1705847 (UMLS CUI [6,1])
C0553723 (UMLS CUI [6,2])
C1522326 (UMLS CUI [6,3])